Synonym(s)
*Sometimes referred to as C. sociale (Guiry 2012).
Classification
(Guiry and Guiry 2012)
Lifestyle
Description
Aperture
"In some diatoms, the space between the valves of adjacent cells in chains" (Horner 2002).
Apertures between cells are long with a slight narrowing in the middle. Spines are thin and arise from just within the CloseMargin
The outline or border that defines the shape of an organism or cell.
margin, three of which are short while the fourth is very long and bundled with the long spines of other cells in the chain. The bundles of long spines from various chains come together in the centre of the colony. One plate-like chloroplast is present per cell and is located in the girdle zone (Cupp 1943). Cells are yellow-brown in colour.Measurements
Apical
(axis, spine) The region of the apex or point. Refers to the most anterior point or region of the cell (HPP 2003).
(apical axis): 2 - 15 μmSmall diameter Close
Transapical axis
In diatoms, the longitudinal axis of the valve.
(transapical axis): 2 - 10 μmLength Close
Pervalvar axis
The axis through the centre point of the two valves of a frustule. This axis is perpendicular to the valve face.
(pervalvar axis): 2 - 12 μm(Kraberg et al. 2010)
Similar species
Harmful effects
Habitat
Distribution
Cosmopolitan (Hasle and Syvertsen 1997), with higher densities in colder waters (Kraberg et al. 2010).
Most abundant in March in northern and Arctic waters (Donnelly 2006). Present from spring to fall, being very abundant in spring in Northern European seas (Kraberg et al. 2010). An important contributor to spring blooms in NE Atlantic and in Artic waters (Degerlund and Eilertsen 2010). Forms blooms in late summer in northern Canadian waters (Booth et al. 2002).
One of the dominant species in late spring in Saanich Inlet, BC (Sancetta and Calvert 1988). Most abundant in early spring and summer off California (Cupp 1943).
Growth conditions
Euphotic
The zone near the surface of the water where the light intensity is sufficient to support net photosynthesis (Letelier et al. 2004). Defined as the area above "the depth at which the photon flux equals 1% of the flux measured just above the air-sea interface" (Ryther 1956).
euphotic zone during low CloseNutrients
Various chemical substances that an organism needs for metabolism (i.e., to live and grow). These are usually taken up from the environment. Some examples include nitrate, phosphate, silica (for diatoms), iron, copper, etc. Some nutrients, like copper, are required for growth, but can also be toxic at high levels.
nutrient conditions, and sinking deeper when nutrients are abundant (Booth et al. 2002). Sensitive to low salinities; usually occurs at salinities of 24 - 34 (Shevchenko et al. 2008). Optimal N:P ratio of 16:1 (Li et al. 1990).Quota
(as in, cell quota for a nutrient) The amount of a macro- or micronutrient required by an organism to fulfill its life cycle.
quota ratio was found to be 3.4 to 4.2 (Iwade et al. 2006).Environmental Ranges
Temperature range (°C): -1.952 - 29.468
Nitrate (μmol L-1): 0.056 - 31.807
Salinity: 18.564 - 37.775
Oxygen (mL L-1): 4.500 - 9.192
Phosphate (μmol L-1): 0.048 - 2.190
Close
Silicic acid
A general term to describe chemical compounds containing silicon, oxygen and hydrogen with a general formula of [SiOx(OH)4-2x]n. Diatoms polymerize silicic acid into biogenic silica to form their frustules (Azam and Chisholm 1976).
Silicate (μmol L-1): 0.754 - 66.097(OBIS 2012, cited in EOL 2012)
Bloom characteristics
References
Booth, B. C., Larouche, P., Bélanger, S., Klein, B., Amiel, D. and Mei, Z. P. 2002. Dynamics of Chaetoceros socialis blooms in the North Water. Deep-Sea Research II. 49: 5003-5025.
Cupp, E. E. 1943. Marine Plankton Diatoms of the West Coast of North America. University of California Press. Berkeley, California. 238.
Degerlund, M. and Eilertsen, H. C. 2010. Main species characteristics of phytoplankton spring blooms in NE Atlantic and Arctic waters (68 - 80° N). Estuaries and Coasts. 33: 242-269.
Donnelly, K. A. M. 2006. The importance of morphological/physiological heterogeneity as adaptive strategies in stocks of common Northern/Arctic phytoplankton species with special focus on the common diatom Chaetoceros socialis. Master's Thesis, University of Tromsø, Norway.
Encyclopedia of Life (EOL). 2012. Chaetoceros socialis. http://eol.org/pages/2540184/overview. Accessed 31 Mar 2012.
Guiry, M. D. 2012. Chaetoceros socialis H. S. Lauder, 1864. http://www.marinespecies.org/aphia.php?p=taxdetails&id=149123. Accessed 31 Mar 2012.
Guiry, M. D. and Guiry, G. M. 2012. Chaetoceros socialis H. S. Lauder. http://www.algaebase.org/search/species/detail/?species_id=37464. Accessed 31 Mar 2012.
Hasle, G. R. and Syvertsen, E. E. 1997. Marine diatoms. In: Tomas, C. R. (ed.) Identifying Marine Phytoplankton. Academic Press, Inc., San Diego. 5-385.
Iwade, S., Kuma, K., Isoda, Y., Yoshida, M., Kudo, I., Nishioka, J. and Suziki, K. 2006. Effect of high iron concentrations on iron uptake and growth of a coastal diatom Chaetoceros sociale. Aquatic Microbial Ecology. 43: 177-191.
Kraberg, A., Baumann, M. and Durselen, C. D. 2010. Coastal Phytoplankton: Photo Guide for Northern European Seas. Verlag Dr. Friedrich Pfeil, Munchen, Germany. 204.
Li, W., Li, S. and Wang, X. 1990. Effects of phosphate on the photosynthetic rate of Chaetoceros socialis. Tropic Oceanology/Redai Haiyang. 9(2): 58-62.
Ocean Biogeographic Information System (OBIS). 2012. Chaetoceros socialis. http://www.iobis.org/mapper/?taxon_id=419717. Accessed 31 Mar 2012.
Shevchenko, O. G., Orlova, T. Y. and Aizdaicher, N. A. 2008. Development of the diatom Chaetoceros socialis f. radians (Schütt) Proschkina-Lavrenko 1963 in laboratory culture. Russian Journal of Marine Biology. 34(4): 224-229.
Sancetta, C. and Calvert, S. E. 1988. The annual cycle of sedimentation in Saanich inlet, British Columbia: implications for the interpretation of diatom fossil assemblages. Deep Sea Research Part A. Oceanographic Research Papers. 35(1): 71-90.